Canonical Allele Identifier: CA2689903660

Gene: NPR2

Linked Data

• gnomAD v4: 9-35800306-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800309_35800310del , CM000671.2:g.35800309_35800310del	GRCh38
NC_000009.11:g.35800306_35800307del , CM000671.1:g.35800306_35800307del	GRCh37
NC_000009.10:g.35790306_35790307del	NCBI36
NG_009249.1:g.12901_12902del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1124-80_1124-79del	ENSP00000402902.2:n.1124-80_1124-79del
ENST00000685871.1:c.1124-80_1124-79del	ENSP00000509964.1:n.1124-80_1124-79del
ENST00000686159.1:n.1163-80_1163-79del
ENST00000687302.1:n.985-80_985-79del
ENST00000687357.1:c.1124-80_1124-79del	ENSP00000509549.1:n.1124-80_1124-79del
ENST00000687625.1:n.279-80_279-79del
ENST00000687787.1:c.1124-80_1124-79del	ENSP00000509440.1:n.1124-80_1124-79del
ENST00000688201.1:n.1156-80_1156-79del
ENST00000688226.1:n.1056-80_1056-79del
ENST00000688869.1:n.1205-80_1205-79del
ENST00000689788.1:c.918-80_918-79del	ENSP00000508973.1:n.918-80_918-79del
ENST00000689898.1:c.1124-80_1124-79del	ENSP00000509651.1:n.1124-80_1124-79del
ENST00000690070.1:c.1124-80_1124-79del	ENSP00000509654.1:n.1124-80_1124-79del
ENST00000690267.1:c.988-80_988-79del	ENSP00000510432.1:n.988-80_988-79del
ENST00000690552.1:n.985-80_985-79del
ENST00000691138.1:n.985-80_985-79del
ENST00000691969.1:c.699-80_699-79del	ENSP00000510244.1:n.699-80_699-79del
ENST00000692232.1:n.1975_1976del
ENST00000692233.1:c.988-80_988-79del	ENSP00000509698.1:n.988-80_988-79del
ENST00000692380.1:n.279-80_279-79del
ENST00000692447.1:n.2236-80_2236-79del
ENST00000693094.1:c.1124-80_1124-79del	ENSP00000510161.1:n.1124-80_1124-79del
ENST00000342694.7:c.1124-80_1124-79del MANE Select	ENSP00000341083.2:n.1124-80_1124-79del
ENST00000342694.6:c.1124-80_1124-79del	ENSP00000341083.2:n.1124-80_1124-79del
ENST00000464810.5:n.1124-80_1124-79del
NM_003995.3:c.1124-80_1124-79del	NP_003986.2:n.1124-80_1124-79del
XM_005251478.3:c.1124-80_1124-79del	XP_005251535.1:n.1124-80_1124-79del
XM_005251479.3:c.137-80_137-79del	XP_005251536.1:n.137-80_137-79del
XM_006716778.2:c.1124-80_1124-79del	XP_006716841.1:n.1124-80_1124-79del
XM_011517889.1:c.137-80_137-79del	XP_011516191.1:n.137-80_137-79del
XM_011517890.1:c.137-80_137-79del	XP_011516192.1:n.137-80_137-79del
XM_011517891.1:c.137-80_137-79del	XP_011516193.1:n.137-80_137-79del
XM_011517892.1:c.137-80_137-79del	XP_011516194.1:n.137-80_137-79del
XM_011517893.1:c.137-80_137-79del	XP_011516195.1:n.137-80_137-79del
XM_011517894.1:c.137-80_137-79del	XP_011516196.1:n.137-80_137-79del
XM_024447556.1:c.1124-80_1124-79del	XP_024303324.1:n.1124-80_1124-79del
XM_024447557.1:c.1124-80_1124-79del	XP_024303325.1:n.1124-80_1124-79del
XM_024447558.1:c.137-80_137-79del	XP_024303326.1:n.137-80_137-79del
XM_024447560.1:c.-285-80_-285-79del	XP_024303328.1:n.-285-80_-285-79del
XM_024447561.1:c.-285-80_-285-79del	XP_024303329.1:n.-285-80_-285-79del
NM_003995.4:c.1124-80_1124-79del MANE Select	NP_003986.2:n.1124-80_1124-79del
NM_001378923.1:c.1124-80_1124-79del	NP_001365852.1:n.1124-80_1124-79del